We describe the synthesis and characterisation of open fullerene (1) and its reduced form (2) in which CH and NH are encapsulated, respectively. The H NMR resonance of endohedral NH is broadened by scalar coupling to the quadrupolar N nucleus, which relaxes rapidly. This broadening is absent for small satellite peaks, which are attributed to natural abundance N. The influence of the scalar relaxation mechanism on the linewidth of the H ammonia resonance is probed by variable temperature NMR. A rotational correlation time of τ =1.5 ps. is determined for endohedral NH , and of τ =57±5 ps. for the open fullerene, indicating free rotation of the encapsulated molecule. IR spectroscopy of NH @2 at 5 K identifies three vibrations of NH (ν , ν and ν ) redshifted in comparison with free NH , and temperature dependence of the IR peak intensity indicates the presence of a large number of excited translational/ rotational states. Variable temperature H NMR spectra indicate that endohedral CH is also able to rotate freely at 223 K, on the NMR timescale. Inelastic neutron scattering (INS) spectra of CH @1 show both rotational and translational modes of CH . Energy of the first excited rotational state (J=1) of CH @1 is significantly lower than that of free CH .
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http://dx.doi.org/10.1002/cphc.201701212 | DOI Listing |
Chem Sci
December 2024
Institut de Quimica Computacional i Catàlisi (IQCC) and Departament de Química, Universitat de Girona M. Aurèlia Capmany, 69 17003 Girona Catalonia Spain
Photodynamic therapy is an important tool in modern medicine due to its effectiveness, safety, and the ability to provide targeted treatment for a range of diseases. Photodynamic therapy utilizes photosensitizers to generate reactive oxygen species (ROS). Fullerenes can be used as photosensitizers to produce ROS in high quantum yields.
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December 2024
Institute for Chemical Research, Kyoto University Gokasho, Uji Kyoto 611-0011 Japan
Although fullerene bisadducts are promising electron-transporting materials for tin halide perovskite solar cells, they are generally synthesized as a mixture of isomeric products that require a complicated separation process. Here, we introduce a phenylene-bridged bis(pyrrolidino)fullerene, Bis-PC, which forms only a single isomer due to geometrical restriction. When used in a tin perovskite solar cell with a PEAFASnI (PEA: phenylethylammonium and FA: formamidinium) light absorption layer, the resulting open-circuit voltage ( ) was 0.
View Article and Find Full Text PDFNanotechnology
December 2024
Institute of Chemistry and Biotechnology, Technical University of Ilmenau, Weimarer Str. 25, Ilmenau, 98693, GERMANY.
The powerful antioxidant properties of C60 fullerenes have been widely used in biomedical nanotechnology. Owing to the negative effects of free radicals in oxidative stress processes, antioxidants are required to protect injured muscles. Here, the effect of water-soluble C60 fullerenes (daily oral dose 1 mg/kg) on the process of restoration of contractile activity of skeletal muscle of rats (muscle gastrocnemius) 15 days after the initiation of open trauma of different severity was studied for the first time.
View Article and Find Full Text PDFChemSusChem
December 2024
School of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou, 341000, P. R. China.
Benzothiadiazole (BT) has shown promising applications in fullerene solar cells. However, few BT-based polymer donors exhibited a noticeable power conversion efficiency (PCE) for the fused-ring small molecular acceptor-based polymer solar cells (PSCs). Herein, we developed a D-A (D: donor, A: acceptor) polymer donor F-1 based on fluorinated BT (ffBT) as A unit and chlorinated benzo [1,2-b : 4,5-b'] dithiophene (BDT-2Cl) as D unit.
View Article and Find Full Text PDFMacromol Rapid Commun
December 2024
Department of Chemistry, Middle East Technical University, Ankara, 06800, Turkey.
Due to their tunable energy levels, ability for intense light absorption, stability and ease of purification, non-fullerene acceptors (NFAs) have significantly contributed to the progress of organic photovoltaics (OPVs). Herein, a series of newly designed and synthesized NFAs specifically tailored are presented for OPV applications. A new class of NFAs possessing carbazole, fluorene, silafluorene derivatives, and benzothiadiazoles are synthesized.
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